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pubmed-article:2292489pubmed:abstractTextCarcinoid tumors which arise from enterochromaffin cells are usually found in the appendix, ileum, bronchus and rectum. Biliary duct carcinoids are exceedingly rare. Pre-operative diagnosis is very difficult because they mimic the signs and symptoms of choledocholithiasis. We report a case of biliary duct carcinoid. A 38-year-old woman admitted with signs and symptoms of obstructive jaundice. ERCP demonstrated an obstruction in the common bile duct. A choledochotomy T drainage was performed. Histopathologically the mass which was removed from the common bile duct was a carcinoid tumor. There are only nine cases of biliary duct carcinoid in the literature to date. These cases are reviewed.lld:pubmed
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pubmed-article:2292489pubmed:authorpubmed-author:OrmeciNNlld:pubmed
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pubmed-article:2292489pubmed:volume75lld:pubmed
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pubmed-article:2292489pubmed:pagination262-4lld:pubmed
pubmed-article:2292489pubmed:dateRevised2009-11-11lld:pubmed
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pubmed-article:2292489pubmed:articleTitleCarcinoid tumor of the biliary duct.lld:pubmed
pubmed-article:2292489pubmed:affiliationDepartment of Surgery, Ankara University Faculty of Medicine, Turkey.lld:pubmed
pubmed-article:2292489pubmed:publicationTypeJournal Articlelld:pubmed
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